AU2005229330B2 - DPP-IV inhibitors - Google Patents
DPP-IV inhibitors Download PDFInfo
- Publication number
- AU2005229330B2 AU2005229330B2 AU2005229330A AU2005229330A AU2005229330B2 AU 2005229330 B2 AU2005229330 B2 AU 2005229330B2 AU 2005229330 A AU2005229330 A AU 2005229330A AU 2005229330 A AU2005229330 A AU 2005229330A AU 2005229330 B2 AU2005229330 B2 AU 2005229330B2
- Authority
- AU
- Australia
- Prior art keywords
- alkyl
- group
- optionally substituted
- independently selected
- halogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- NKMBCTDYIIRIKW-UHFFFAOYSA-N tert-butyl n-[(2-fluorophenyl)methyl]carbamate Chemical compound CC(C)(C)OC(=O)NCC1=CC=CC=C1F NKMBCTDYIIRIKW-UHFFFAOYSA-N 0.000 description 1
- DJLHLEHLARTHPF-UHFFFAOYSA-N tert-butyl n-[(2-methylsulfinylphenyl)methyl]carbamate Chemical compound CS(=O)C1=CC=CC=C1CNC(=O)OC(C)(C)C DJLHLEHLARTHPF-UHFFFAOYSA-N 0.000 description 1
- IOMPSERRLKOLIN-GOSISDBHSA-N tert-butyl n-[(2r)-1-(2-fluorophenyl)-4-[(2-fluorophenyl)methyl-methylamino]-4-oxobutan-2-yl]carbamate Chemical compound C([C@@H](CC=1C(=CC=CC=1)F)NC(=O)OC(C)(C)C)C(=O)N(C)CC1=CC=CC=C1F IOMPSERRLKOLIN-GOSISDBHSA-N 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical class CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 1
- WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
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- ZYXWYDDFNXBTFO-UHFFFAOYSA-N tetrazolidine Chemical compound C1NNNN1 ZYXWYDDFNXBTFO-UHFFFAOYSA-N 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 230000004797 therapeutic response Effects 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- RLTPJVKHGBFGQA-UHFFFAOYSA-N thiadiazolidine Chemical compound C1CSNN1 RLTPJVKHGBFGQA-UHFFFAOYSA-N 0.000 description 1
- 150000001467 thiazolidinediones Chemical class 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 210000001541 thymus gland Anatomy 0.000 description 1
- 229960005371 tolbutamide Drugs 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- GXPHKUHSUJUWKP-UHFFFAOYSA-N troglitazone Chemical compound C1CC=2C(C)=C(O)C(C)=C(C)C=2OC1(C)COC(C=C1)=CC=C1CC1SC(=O)NC1=O GXPHKUHSUJUWKP-UHFFFAOYSA-N 0.000 description 1
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- GXPHKUHSUJUWKP-NTKDMRAZSA-N troglitazone Natural products C([C@@]1(OC=2C(C)=C(C(=C(C)C=2CC1)O)C)C)OC(C=C1)=CC=C1C[C@H]1SC(=O)NC1=O GXPHKUHSUJUWKP-NTKDMRAZSA-N 0.000 description 1
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Classifications
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- C07D311/76—Benzo[c]pyrans
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- C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
- C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D319/18—Ethylenedioxybenzenes, not substituted on the hetero ring
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
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- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04005347A EP1593671A1 (fr) | 2004-03-05 | 2004-03-05 | Inhibiteurs de la DPP-IV |
EP04005347.2 | 2004-03-05 | ||
PCT/EP2005/002010 WO2005095343A1 (fr) | 2004-03-05 | 2005-02-25 | Inhibiteurs de la dpp-iv |
Publications (2)
Publication Number | Publication Date |
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AU2005229330A1 AU2005229330A1 (en) | 2005-10-13 |
AU2005229330B2 true AU2005229330B2 (en) | 2008-12-18 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2005229330A Expired - Fee Related AU2005229330B2 (en) | 2004-03-05 | 2005-02-25 | DPP-IV inhibitors |
Country Status (11)
Country | Link |
---|---|
US (1) | US20070197522A1 (fr) |
EP (2) | EP1593671A1 (fr) |
JP (1) | JP2007526267A (fr) |
KR (1) | KR20070007816A (fr) |
CN (1) | CN1980892A (fr) |
AU (1) | AU2005229330B2 (fr) |
CA (1) | CA2558446A1 (fr) |
MX (1) | MXPA06010097A (fr) |
NO (1) | NO20064032L (fr) |
RU (1) | RU2345067C2 (fr) |
WO (1) | WO2005095343A1 (fr) |
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DE102004054054A1 (de) | 2004-11-05 | 2006-05-11 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verfahren zur Herstellung chiraler 8-(3-Amino-piperidin-1-yl)-xanthine |
PE20061156A1 (es) | 2004-12-23 | 2006-12-16 | Glaxo Group Ltd | Derivados de benzamida como agentes inhibidores del transportador de glicina |
DE102005035891A1 (de) | 2005-07-30 | 2007-02-08 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel |
WO2007063928A1 (fr) * | 2005-11-30 | 2007-06-07 | Toray Industries, Inc. | Nouveau derive non cyclique d’amine carboxamide et sel de celui-ci |
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DK4069360T3 (da) | 2019-12-04 | 2024-02-26 | Albireo Ab | Benzothia(di)azepinforbindelser og anvendelse deraf som galdesyremodulatorer |
EP4069361B1 (fr) | 2019-12-04 | 2024-01-03 | Albireo AB | Composés de benzothia(di)azépine et leur utilisation en tant que modulateurs de l'acide biliaire |
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US5455271A (en) * | 1992-06-18 | 1995-10-03 | The Scripps Research Institute | Tight-binding inhibitors of leukotriene A4 hydrolase |
DE122010000020I1 (de) * | 1996-04-25 | 2010-07-08 | Prosidion Ltd | Verfahren zur Senkung des Blutglukosespiegels in Säugern |
DE60224189T2 (de) * | 2001-06-20 | 2008-12-11 | Merck & Co., Inc. | Dipeptidylpeptidase-hemmer zur behandlung von diabetes |
ES2257555T3 (es) * | 2001-06-20 | 2006-08-01 | MERCK & CO., INC. | Inhibidores de dipeptidilpeptidasa para el tratamiento de la diabetes. |
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2004
- 2004-03-05 EP EP04005347A patent/EP1593671A1/fr not_active Withdrawn
-
2005
- 2005-02-25 MX MXPA06010097A patent/MXPA06010097A/es unknown
- 2005-02-25 WO PCT/EP2005/002010 patent/WO2005095343A1/fr active Application Filing
- 2005-02-25 CA CA002558446A patent/CA2558446A1/fr not_active Abandoned
- 2005-02-25 KR KR1020067020710A patent/KR20070007816A/ko active Application Filing
- 2005-02-25 CN CNA2005800137836A patent/CN1980892A/zh active Pending
- 2005-02-25 RU RU2006131597/04A patent/RU2345067C2/ru not_active IP Right Cessation
- 2005-02-25 US US10/591,108 patent/US20070197522A1/en not_active Abandoned
- 2005-02-25 JP JP2007501183A patent/JP2007526267A/ja not_active Withdrawn
- 2005-02-25 EP EP05715551A patent/EP1758861A1/fr not_active Withdrawn
- 2005-02-25 AU AU2005229330A patent/AU2005229330B2/en not_active Expired - Fee Related
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2006
- 2006-09-07 NO NO20064032A patent/NO20064032L/no not_active Application Discontinuation
Patent Citations (1)
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WO2004085378A1 (fr) * | 2003-03-19 | 2004-10-07 | Merck & Co. Inc. | Procede pour preparer des derives d'acide amine beta chiraux par hydrogenation asymetrique |
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Journal of the American Chemical Society, 125(27): 8090-91, 6 November 2003 * |
Tetrahedron Letters, 37(47): 8589-8592, 1996 * |
Tetrahedron Letters, 44(40): 7537-40, 29 September 2003 * |
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RU2345067C2 (ru) | 2009-01-27 |
US20070197522A1 (en) | 2007-08-23 |
NO20064032L (no) | 2006-11-08 |
RU2006131597A (ru) | 2008-04-10 |
EP1593671A1 (fr) | 2005-11-09 |
MXPA06010097A (es) | 2007-06-15 |
WO2005095343A1 (fr) | 2005-10-13 |
AU2005229330A1 (en) | 2005-10-13 |
CA2558446A1 (fr) | 2005-10-13 |
CN1980892A (zh) | 2007-06-13 |
JP2007526267A (ja) | 2007-09-13 |
KR20070007816A (ko) | 2007-01-16 |
EP1758861A1 (fr) | 2007-03-07 |
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